Team:DTU-Denmark/Notebook/9 July 2013

From 2013.igem.org

(Difference between revisions)
(→Main purpose)
 
(23 intermediate revisions not shown)
Line 1: Line 1:
-
=208=
+
{{:Team:DTU-Denmark/Templates/StartPage|9 July 2013}}
 +
Navigate to the [[Team:DTU-Denmark/Notebook/8_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/10_July_2013|Next]] Entry
 +
=Lab 208=
 +
<hr/>
==Main purpose==
==Main purpose==
 +
<hr/>
Run gel with 7 PCR samples of Nir operon from ''Pseudomonas aeruginosa'' and purified AMO, HAO and CYC from 08.07.2013.
Run gel with 7 PCR samples of Nir operon from ''Pseudomonas aeruginosa'' and purified AMO, HAO and CYC from 08.07.2013.
Line 8: Line 12:
==Who was in the lab==
==Who was in the lab==
-
Ariadni,Henrike,Julia
+
<hr/>
 +
Ariadni, Henrike, Julia, Gosia
==Procedure==
==Procedure==
-
 
+
<hr/>
===Run gel===
===Run gel===
===Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)===
===Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)===
-
===PCR===
+
===Extraction PCR===
 +
to produce the right fragment of the Nir operon from either chromosomal DNA from ''Pseudomonas aeruginosa'' or the too long PCR fragments from the 08.07.
 +
 
 +
6 samples
 +
 
 +
*3 samples from culture pAO1
 +
*3 samples from today's purification of the PCR that was done on 08.07.
 +
master mix for 7 reactions
 +
* dNTP: 1 ul (7 ul)
 +
* HF buffer: 10 ul (70 ul)
 +
* Phusion polymerase: 0.5 ul (3.5 ul)
 +
* H<sub>2</sub>O: 31.5 ul (220.5 ul)
 +
 
 +
Settings for PCR
 +
{| class="wikitable" style="text-align: right"
 +
! Temperature (<sup>o</sup>C)!! Time (min)!! Rounds
 +
|-
 +
| 98 || 2:00 || 1
 +
|-
 +
| 98 || 0:20 || 35
 +
|-
 +
| 66 || 0:45 || 35
 +
|-
 +
| 72 || 9:00 || 35
 +
|-
 +
| 72 || 5:00 || 1
 +
|-
 +
| 4|| ∞ || -
 +
|}
==Results==
==Results==
-
Nanodrop measurement:
+
<hr/>
-
*  ng/ul (Nir)
+
Nanodrop measurement of Nir operon:
-
*  ng/ul (Nir)
+
*  17.98 ng/ul  
-
*  ng/ul (Nir)
+
*  16.82 ng/ul  
 +
*  8.51 ng/ul
 +
 
 +
Navigate to the [[Team:DTU-Denmark/Notebook/8_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/10_July_2013|Next]] Entry
 +
 
 +
{{:Team:DTU-Denmark/Templates/EndPage}}

Latest revision as of 20:39, 16 September 2013

9 July 2013

Navigate to the Previous or the Next Entry

Contents

Lab 208

Main purpose

Run gel with 7 PCR samples of Nir operon from Pseudomonas aeruginosa and purified AMO, HAO and CYC from 08.07.2013.

Purification of Nir operon and Nanodrop measurement.

Set up new PCR reaction to extract Nir from Pseudomonas aeruginosa.

Who was in the lab

Ariadni, Henrike, Julia, Gosia

Procedure

Run gel

Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)

Extraction PCR

to produce the right fragment of the Nir operon from either chromosomal DNA from Pseudomonas aeruginosa or the too long PCR fragments from the 08.07.

6 samples

  • 3 samples from culture pAO1
  • 3 samples from today's purification of the PCR that was done on 08.07.

master mix for 7 reactions

  • dNTP: 1 ul (7 ul)
  • HF buffer: 10 ul (70 ul)
  • Phusion polymerase: 0.5 ul (3.5 ul)
  • H2O: 31.5 ul (220.5 ul)

Settings for PCR

Temperature (oC) Time (min) Rounds
98 2:00 1
98 0:20 35
66 0:45 35
72 9:00 35
72 5:00 1
4 ∞ -

Results

Nanodrop measurement of Nir operon:

  • 17.98 ng/ul
  • 16.82 ng/ul
  • 8.51 ng/ul

Navigate to the Previous or the Next Entry

Retrieved from "http://2013.igem.org/Team:DTU-Denmark/Notebook/9_July_2013"